Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 1 - 10 of 659 for 11S -"8-CHLORO-11-[1-(METHYLSULFONYL)PIPERIDIN-4-YL]-6-PIPERAZIN-1-YL-11H-BENZO[5,6]CYCLOHEPTA[1,2-B]PYRIDINE"
Did you mean 11S -"8-CHLORO-11-[1-(METHYLSULFONYL)picaridin-4-YL]-6-PIPERAZIN-1-YL-11H-benz[5,6]CYCLOHEPTA[1,2-B]PYRIDINE"?
  1. Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency 
    Congenital adrenal hyperplasia (CAH) due to 11-beta-hydroxylase deficiency is one of a group of disorders (collectively called congenital adrenal hyperplasia) that ...
    https://medlineplus.gov/...sia-due-to-11-beta-hydroxylase-deficiency - Genetics
  2. Spastic paraplegia type 11 
    Spastic paraplegia type 11 is part of a group of genetic disorders known as hereditary spastic paraplegias. These disorders are characterized by progressive ...
    https://medlineplus.gov/.../condition/spastic-paraplegia-type-11 - Genetics
  3. Myoclonus-dystonia 
    ... condition can be inherited from either parent. Dystonia 11 DYT11 Myoclonus-dystonia syndrome Genetic Testing Registry: Myoclonic dystonia 11 Myoclonus-dystonia syndrome National Organization for Rare Disorders ( ...
    https://medlineplus.gov/genetics/condition/myoclonus-dystonia - Genetics
  4. Emanuel syndrome 
    ... the presence of extra genetic material from chromosome 11 and chromosome 22 in each cell. In addition ... supernumerary) chromosome consisting of a piece of chromosome 11 attached to a piece of chromosome 22. The ...
    https://medlineplus.gov/genetics/condition/emanuel-syndrome - Genetics
  5. Fundus albipunctatus 
    ... cycle is the recycling of a molecule called 11-cis retinal, which is a form of vitamin ... gene provides instructions for making an enzyme called 11-cis retinol dehydrogenase 5, which performs one step ...
    https://medlineplus.gov/genetics/condition/fundus-albipunctatus - Genetics
  6. Jacobsen syndrome 
    ... a loss (deletion) of genetic material from chromosome 11. Because this deletion most commonly occurs at the ... terminus) of the long (q) arm of chromosome 11, Jacobsen syndrome is also known as 11q terminal ...
    https://medlineplus.gov/genetics/condition/jacobsen-syndrome - Genetics
  7. Glycoprotein VI deficiency 
    ... a collagen receptor defect Bleeding disorder, platelet-type, 11 GP VI deficiency Genetic Testing Registry: Platelet-type bleeding disorder 11 Bleeding diathesis due to glycoprotein VI deficiency National ...
    https://medlineplus.gov/.../condition/glycoprotein-vi-deficiency - Genetics
  8. Factor XI deficiency 
    ... does not run in families. F11 deficiency Factor 11 deficiency Haemophilia C Hemophilia C Plasma thromboplastin antecedent ... 541-50. doi: 10.1016/j.thromres.2011.11.051. Epub 2011 Dec 22. Citation on PubMed ...
    https://medlineplus.gov/genetics/condition/factor-xi-deficiency - Genetics
  9. 21-hydroxylase deficiency 
    21-hydroxylase deficiency is an inherited disorder that affects the adrenal glands. The adrenal glands are located on top of the kidneys and produce a variety ...
    https://medlineplus.gov/genetics/condition/21-hydroxylase-deficiency - Genetics
  10. Beckwith-Wiedemann syndrome 
    ... of genes in a particular region of chromosome 11. People normally inherit one copy of this chromosome from each parent. For most genes on chromosome 11, both copies of the gene are expressed, or " ...
    https://medlineplus.gov/.../condition/beckwith-wiedemann-syndrome - Genetics
previous · 1 · 2 · 3 · 4 · 5 · 6 · 7 · 8 · 9 · 10 · next